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Frequency of four cystic fibrosis mutations in a Swedish population

1993; Wiley; Volume: 82; Issue: 6-7 Linguagem: Inglês

10.1111/j.1651-2227.1993.tb12769.x

1651-2227

Niklas Dahl, Ulla Grandell, Tommy Martinsson, Marie Allen, Lena Johansson, Lisa Stolpe, Ulf Gyllensten, Lena Hjelte, H Kollberg, Birgitta Strandvik, J. Wahlström, Maria Anvret,

Neonatal Respiratory Health Research

Acta PaediatricaVolume 82, Issue 6-7 p. 609-609 Frequency of four cystic fibrosis mutations in a Swedish population N Dahl, N Dahl 1Department of Medical GeneticsSearch for more papers by this authorU Grandell, U Grandell Biochemical Centre, Uppsula, Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorT Martinsson, T Martinsson Kurolinska Hospital, Stockholm. Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorM Allen, M Allen 1Department of Medical GeneticsSearch for more papers by this authorL Johansson, L Johansson Biochemical Centre, Uppsula, Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorL Stolpe, L Stolpe Biochemical Centre, Uppsula, Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorU Gyllensten, U Gyllensten 1Department of Medical GeneticsSearch for more papers by this authorL Hjelte, L Hjelte Östra Hospital, Göteborg. Department of Pediatrics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorH Kollberg, H Kollberg Huddinge Hospital. Stockholm. Department of Pediatrics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorB Strandvik, B Strandvik Umeå University Hospital. Umeå and Department of Pediatrics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorJ Wahlstrom, J Wahlstrom Kurolinska Hospital, Stockholm. Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorM Anvret, M Anvret Biochemical Centre, Uppsula, Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this author N Dahl, N Dahl 1Department of Medical GeneticsSearch for more papers by this authorU Grandell, U Grandell Biochemical Centre, Uppsula, Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorT Martinsson, T Martinsson Kurolinska Hospital, Stockholm. Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorM Allen, M Allen 1Department of Medical GeneticsSearch for more papers by this authorL Johansson, L Johansson Biochemical Centre, Uppsula, Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorL Stolpe, L Stolpe Biochemical Centre, Uppsula, Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorU Gyllensten, U Gyllensten 1Department of Medical GeneticsSearch for more papers by this authorL Hjelte, L Hjelte Östra Hospital, Göteborg. Department of Pediatrics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorH Kollberg, H Kollberg Huddinge Hospital. Stockholm. Department of Pediatrics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorB Strandvik, B Strandvik Umeå University Hospital. Umeå and Department of Pediatrics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorJ Wahlstrom, J Wahlstrom Kurolinska Hospital, Stockholm. Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this authorM Anvret, M Anvret Biochemical Centre, Uppsula, Department of Clinical Genetics Östra Hospital, Göteborg, Sweden. Corresponding author M AnvretSearch for more papers by this author First published: June 1993 https://doi.org/10.1111/j.1651-2227.1993.tb12769.xCitations: 5AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1 Riordan Jr, Rommens JM, Kerem Bs et al.. Identification of the cystic fibrosis gene: cloning and charcterization of complementary DNA. Science 1989; 245: 1066–73. 10.1126/science.2475911 CASPubMedWeb of Science®Google Scholar 2 Rommens J Lannuzzi MC, Kerem BS et al.. 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Hum Genet 1990; 84: 449–54. 10.1007/BF00195818 CASPubMedWeb of Science®Google Scholar Citing Literature Volume82, Issue6-7June 1993Pages 609-609 ReferencesRelatedInformation